Zobrazeno 1 - 10
of 124
pro vyhledávání: '"K M, Call"'
Autor:
K. M. Call, Charis Eng, Shikha Bose, Ramon Parsons, Patricia L. M. Dahia, Jing Li, Deborah J. Marsh, Steven I. Wang, Z. Zheng, Danny Liaw, Hui C. Tsou, Monica Peacocke
Publikováno v:
Scopus-Elsevier
Cowden disease (CD) is an autosomal dominant cancer predisposition syndrome associated with an elevated risk for tumours of the breast, thyroid and skin1–2. Lhermitte-Duclos disease (LDD) cosegregates with a subset of CD families and is associated
Autor:
P R, August, T H, Grossman, C, Minor, M P, Draper, I A, MacNeil, J M, Pemberton, K M, Call, D, Holt, M S, Osburne
Publikováno v:
Journal of molecular microbiology and biotechnology. 2(4)
Violacein is a purple-colored, broad-spectrum antibacterial pigment that has a dimeric structure composed of 5-hydroxyindole, oxindole and 2-pyyrolidone subunits formed by the condensation of two modified tryptophan molecules. The violacein biosynthe
Autor:
D J, Marsh, P L, Dahia, V, Coulon, Z, Zheng, F, Dorion-Bonnet, K M, Call, R, Little, A Y, Lin, R A, Eeles, A M, Goldstein, S V, Hodgson, A L, Richardson, B G, Robinson, H C, Weber, M, Longy, C, Eng
Publikováno v:
Genes, chromosomescancer. 21(1)
Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the pr
Publikováno v:
Cell growthdifferentiation : the molecular biology journal of the American Association for Cancer Research. 5(6)
Evidence implicates the product of the Wilms' tumor suppressor gene, WT1, in proliferation and differentiation of target tissues during development. Study of the regulation of other tumor suppressor genes during these processes has been instrumental
Publikováno v:
Oncogene. 6(4)
We have analysed 55 Wilms' tumour DNAs using the cDNA from the candidate Wilms' predisposition gene, WT1. One tumour, GOS 129, shows a partial homozygous deletion involving only the 3'-most exon of the gene. An adjacent 3' DNA sequence, J7-18, which
Autor:
Adel, Marim1 (AUTHOR), Chung, Joanne M.2 (AUTHOR)
Publikováno v:
European Journal of Personality. Oct2024, p1.
Publikováno v:
Cancer research. 47(8)
Diploid human lymphoblast cells exhibit apparent saturation of mutation induced by exposure to aflatoxin B1, despite a linear increase in the amount and proportion of the aflatoxin-DNA adducts formed. The saturation is neither a cell cycle phenomenon
Publikováno v:
IOP Conference Series: Earth & Environmental Science; 2024, Vol. 1338 Issue 1, p1-8, 8p
Autor:
Frömmel, Michael1 (AUTHOR) michael.froemmel@ugent.be, Kadioglu, Eyup1,2 (AUTHOR)
Publikováno v:
Financial Innovation. 7/21/2023, Vol. 9 Issue 1, p1-23. 23p.
Autor:
Lyski, Zoe L.1 (AUTHOR), Kim, Myung Sun2 (AUTHOR), Xthona Lee, David1 (AUTHOR), Sampson, David2 (AUTHOR), Raué, Hans-Peter3 (AUTHOR), Raghunathan, Vikram2 (AUTHOR), Ryan, Debbie2 (AUTHOR), Brunton, Amanda E.4 (AUTHOR), Slifka, Mark K.3 (AUTHOR), Messer, William B.1,3,5 (AUTHOR), Spurgeon, Stephen E.2 (AUTHOR)
Publikováno v:
Case Reports in Hematology. 2/4/2022, p1-5. 5p.